N-(2-bromophenyl)cinnamamide is an organic compound characterized by its structure, which features a cinnamamide backbone substituted with a 2-bromophenyl group. This compound typically exhibits a solid state at room temperature and is likely to be a pale yellow to off-white crystalline substance. The presence of the bromine atom introduces notable electronegative characteristics, influencing its reactivity and potential interactions with other chemical species. The amide functional group contributes to its ability to engage in hydrogen bonding, which can affect its solubility in various solvents. N-(2-bromophenyl)cinnamamide may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its synthesis often involves coupling reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, this compound represents a unique intersection of aromatic chemistry and functional group reactivity, making it a subject of interest in both academic and industrial research contexts.

N-(2-bromophenyl)cinnamamide

71910-51-5: N-(2-bromophenyl)cinnamamide is an organic compound characterized by its structure, which features a cinnamamide backbone substituted with a 2-bromophenyl group. This compound typically exhibits a solid state at room temperature and is likely to be a pale yellow to off-white crystalline substance. The presence of the bromine atom introduces notable electronegative characteristics, influencing its reactivity and potential interactions with other chemical species. The amide functional group contributes to its ability to engage in hydrogen bonding, which can affect its solubility in various solvents. N-(2-bromophenyl)cinnamamide may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its synthesis often involves coupling reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, this compound represents a unique intersection of aromatic chemistry and functional group reactivity, making it a subject of interest in both academic and industrial research contexts.

CAS 71910-51-5

N-(2-bromophenyl)cinnamamide

N-(2-Bromophenyl)-3-Phenylprop-2-Enamide

Ref: IN-DA00FBB2

N-(2-Bromophenyl)-3-Phenylprop-2-Enamide

Ref: 54-OR1013955